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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5455139copy number variation1nstd206human GRCh38 chr6: 83,191,861-83,192,156 , GRCh37.p13 chr6: 83,901,580-83,901,875 PGM3, RWDD2A
    nsv5381391copy number variation1nstd102humanUncertain significance GRCh37 chr6: 83,878,953-84,567,108 , GRCh38.p12 chr6: 83,169,234-83,857,389 DOP1A, LOC105377879, 6 more genes
    nsv5369371translocation1nstd200human GRCh38 chr6: 83,191,890-83,191,890 , GRCh38 chr6: 83,192,136-83,192,136 , GRCh37.p13 chr6: 83,901,855-83,901,855 , GRCh37.p13 chr6: 83,901,609-83,901,609 RWDD2A, PGM3
    nsv5337374translocation1nstd200human GRCh37 chr6: 83,901,855-83,901,855 , GRCh37 chr6: 83,901,609-83,901,609 , GRCh38.p12 chr6: 83,191,890-83,191,890 , GRCh38.p12 chr6: 83,192,136-83,192,136 RWDD2A, PGM3
    nsv5315135copy number variation1nstd204human GRCh37.p13 chr6: 83,751,730-83,906,773 , GRCh38.p13 chr6: 83,042,011-83,197,054 PGM3, DOP1A, 2 more genes
    nsv5235293copy number variation1nstd204human GRCh38.p13 chr6: 83,193,242-83,194,241 , GRCh37.p13 chr6: 83,902,961-83,903,960 PGM3, RWDD2A
    nsv4941868copy number variation1nstd200human GRCh38 chr6: 83,089,224-83,341,439 , GRCh37.p13 chr6: 83,798,943-84,051,158 ME1, PGM3, 2 more genes
    nsv4816776copy number variation1nstd200human GRCh37 chr6: 83,751,736-83,906,764 , GRCh38.p12 chr6: 83,042,017-83,197,045 PGM3, RWDD2A, 2 more genes
    nsv4675056copy number variation1nstd102humanUncertain significance GRCh37 chr6: 82,620,262-84,201,117 , GRCh38.p12 chr6: 81,910,545-83,491,398 LOC100132659, DOP1A, 14 more genes
    nsv4607045copy number variation1nstd183human GRCh37 chr6: 83,903,097-83,903,173 , GRCh38.p12 chr6: 83,193,378-83,193,454 RWDD2A, PGM3
    nsv4455848copy number variation1nstd102humanUncertain significance GRCh37 chr6: 82,987,696-84,007,694 , GRCh38.p12 chr6: 82,277,979-83,297,975 LOC105377876, DOP1A, 8 more genes
    nsv4148095copy number variation1nstd166human GRCh37.p13 chr6: 83,901,609-83,901,855 , GRCh38.p12 chr6: 83,191,890-83,192,136 RWDD2A, PGM3
    nsv4148019copy number variation1nstd166human GRCh37.p13 chr6: 83,901,610-83,901,961 , GRCh38.p12 chr6: 83,191,891-83,192,242 RWDD2A, PGM3
    nsv3924180copy number variation1nstd102humanPathogenic NCBI36 chr6: 65,316,269-84,193,229 , GRCh38 chr6: 64,549,655-83,426,791 , GRCh37 chr6: 65,259,548-84,136,510 LOC105377875, KCNQ5-IT1, 188 more genes
    nsv3921478copy number variation1nstd102humanPathogenic NCBI36 chr6: 76,692,636-93,477,232 , GRCh38 chr6: 75,926,199-92,710,793 , GRCh37 chr6: 76,635,916-93,420,511 SPACA1, TAF13P1, 187 more genes
    nsv3919111copy number variation1nstd102humanPathogenic GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637 RNU6-770P, MAP3K5-AS2, 810 more genes
    nsv3914309copy number variation1nstd102humanPathogenic GRCh38 chr6: 82,569,098-93,753,476 , NCBI36 chr6: 83,335,534-94,519,915 , GRCh37 chr6: 83,278,815-94,463,194 ME1, GJB7, 136 more genes
    nsv3911622copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 79,678,455-84,862,865 , GRCh37.p13 chr6: 79,621,736-84,806,146 , GRCh38.p12 chr6: 78,912,019-84,096,427 BCKDHB, DBIP1, 55 more genes
    nsv3889959copy number variation1nstd102humanPathogenic GRCh37 chr6: 73,674,612-84,829,774 , GRCh38.p12 chr6: 72,964,889-84,120,055 MRAP2, LCA5, 125 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
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